Iron-Catalyzed Selective Sulfonylation of Alkenes by Sulfonyl Chlorides

Herein, we report an iron-catalyzed approach for the generation of sulfonyl radicals from readily available bulk raw material sulfonyl chlorides and selective sulfonylation of alkenes for the synthesis of β-keto sulfones and vinyl sulfones depending on the reaction conditions. Under mild aerobic oxidation conditions in ethanol, β-keto sulfones were obtained via C(sp<sup>2</sup>)-C bond cleavage, while under argon protection in hexafluoroisopropanol, vinyl sulfones were formed. Mechanism studies reveal that iron salts play the role of hitting two birds with one stone, involving hydrogen atom transfer (HAT) and single-electron transfer (SET) processes.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-17
DOI
https://doi.org/10.1021/acs.joc.5c01566
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Iron-Catalyzed Selective Sulfonylation of Alkenes by Sulfonyl Chlorides

Qiang Bian, Da‐Zhen Xu, Tong‐Tong Zhao, Ziyu Liu et al.
1 citations
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
0.94
article

Iron-Catalyzed Selective Sulfonylation of Alkenes by Sulfonyl Chlorides

Qiang Bian, Da‐Zhen Xu, Tong‐Tong Zhao, Ziyu Liu, Keyu Li, Si-Han Zheng, Shuhan Wang
article en
1 citations

Abstract

Herein, we report an iron-catalyzed approach for the generation of sulfonyl radicals from readily available bulk raw material sulfonyl chlorides and selective sulfonylation of alkenes for the synthesis of β-keto sulfones and vinyl sulfones depending on the reaction conditions. Under mild aerobic oxidation conditions in ethanol, β-keto sulfones were obtained via C(sp<sup>2</sup>)-C bond cleavage, while under argon protection in hexafluoroisopropanol, vinyl sulfones were formed. Mechanism studies reveal that iron salts play the role of hitting two birds with one stone, involving hydrogen atom transfer (HAT) and single-electron transfer (SET) processes.

The Journal of Organic ChemistryVol. 90(44)
Harbin Institute of Technology (CN), Nankai University (CN), Beijing Satellite Navigation Center (CN), Institute of Navigation (US)
Openalex Percentile: Top 21%
Sulfur-Based Synthesis Techniques
0.94
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